Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3039411298

FEI Number

3039411298

Entity Name

AURALITY INC.

City/State/Country

Herndon, VA, US

Establishment Address

580 Herndon Pkwy., Ste 350, Herndon, VA 20170, US

Establishment Type(s)

Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Aurality Inc. (Owner Number: 10094787)

Owner / Operator Contact Address

580 Herndon Pkwy., Ste 350, Herndon, VA 20170, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Empress3D Auditory Canal Scanner

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2025-12-23

Official Correspondent

Mathieu Aubailly

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aurality Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039411298. Last updated year: 2026. Please use registration number 3039411298 when referencing this establishment in official correspondence.